The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
113182897 11318289 7 F 20150526 20160721 20150728 20160725 EXP PHHY2015AU073991 NOVARTIS 87.42 YR M Y 0.00000 20160725 OT AU AU

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
113182897 11318289 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 10 MG, UNK 346714 21008 10 MG
113182897 11318289 2 C PANADOL ACETAMINOPHEN 1 Unknown UNK 0
113182897 11318289 3 C TARGIN NALOXONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113182897 11318289 1 Neuroendocrine tumour
113182897 11318289 2 Product used for unknown indication
113182897 11318289 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
113182897 11318289 OT
113182897 11318289 HO
113182897 11318289 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
113182897 11318289 Anaemia
113182897 11318289 Chest pain
113182897 11318289 Dizziness
113182897 11318289 Dysphagia
113182897 11318289 Feeling abnormal
113182897 11318289 Full blood count decreased
113182897 11318289 Malaise
113182897 11318289 Myelodysplastic syndrome
113182897 11318289 Second primary malignancy
113182897 11318289 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
113182897 11318289 1 20141103 0